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Yes-associated protein promotes cell proliferation by activating Fos Related Activator-1 in oral squamous cell carcinoma

机译:通过在口腔鳞状细胞癌中激活FOS相关活化剂-1,均相关蛋白质促进细胞增殖

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In our previous study, we established an in vitro cellular carcinogenesis model of oral squamous cell carcinoma (OSCC), including a human immortalized oral epithelial cell (HIOEC) and a cancerous cell line (HB96). Microarray analysis showed that the gene encoding Yes-associated protein (YAP) was significantly increased in HB96 cells compared with HIOEC cells. But the underlying mechanism of YAP on oncogenesis, especially its downstream targets, are still not clear. YAP expression in OSCC cell lines and tissue specimens were investigated by using realtime PCR. western blotting and immunohistochem-istry staining. YAP put-back plasmid with four mutation sites after YAP-siRNA interference was constructed by site-directed muugenesis. Cell growth and colony formation were observed after YAP-siRNA interference or YAP put-back again in CAL27 cells. YAP expression was increased in the cellular carcinogenesis models and the clinical samples from primary OSCC patients. Inhibition of YAP by siRNA interference in CAL27 cells significantly inhibited cell proliferation and colony formation in soft agar. but these abilities were rescued when YAP was put-back again. At the same time, Fos Related Activator-1 (Fra-1) was downregulated when YAP was inhibited by siRNA interference while Fra-1 was rescued when YAP was put-back again. Immunohistochemistry results also indicated that higher levels of YAP were significantly associated with Fra-1 overexpression in OSCC clinical samples. YAP could promote cell proliferation by activating transcription factor Fra1 in oral squamous cell carcinoma.
机译:在我们以前的研究中,我们建立了口腔鳞状细胞癌(OSCC)的体外细胞致癌模型,包括人造永生的口腔上皮细胞(HB96)和癌细胞系(HB96)。微阵列分析表明,与HB96细胞相比,编码是相关蛋白(YAP)的基因在与HB96细胞中显着增加。但是yap对肿瘤发生的潜在机制,尤其是下游目标,仍然不明确。通过使用Realtime PCR研究了OSCC细胞系和组织标本中的YAP表达。 Western Blotting和免疫组织学患染色。 Yap-siRNA干扰后具有四个突变位点的yap浸渍质粒由位点定向的Mugenesis构建。在CAL27细胞中再次再次浸洗后观察到细胞生长和菌落形成。在细胞致癌模型和原发性OSCC患者的临床样本中增加了YAP表达。通过SiRNA干扰抑制CAL27细胞的抑制显着抑制了软琼脂中的细胞增殖和菌落形成。但是,当yap再次被恢复时,这些能力被救出。同时,当通过siRNA干扰抑制yap抑制yap时,在yap被扣除时再次恢复yap时,将下调FOS相关活化剂-1(FRA-1)。免疫组织化学结果也表明,较高水平的yap与OSCC临床样品中的FRA-1过表达显着相关。 YAP可以通过激活口腔鳞状细胞癌中的转录因子FRA1来促进细胞增殖。

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